Enroll for the low cost clinical training Phase Trials1,2,3,4ICH-GCPClinical Trial ProcessBA,BE StudiesResponsibilities of Clinical Research PersonsPK,PDCTMsRegulatory Bodies(FDA,IRB,NDA)Clinical Research DocumentsClinical Data Management Training (Especially Present Industry Expected)protocolunderstanding Of ProtocolElectronic CRF DesigningEdit Check ProgrammingEdit Checks ImplementationData Base..
Training offeringsWe are starting our exclusive sessions on SAS Clinical training. Classes are available on weekend and weekdays. Please call us immediately to reserve your seats and for details. Training Highlights100% Placement for Committed Candidates for best performers (Post Evaluation )Industry Expertise excellent Mentors on different technologies, and domainsExcellent trainers with decades ..
Hi,We provide SAS clinical Programming training from the Expert in SAS clinical programming.You can attend the real time Project with hands on exp in SAS clinical programming.Will be trained fully for the SAS Clinical Certification programSAS Clinical (Base SAS, Advance SAS and Biostatistics) Features:* Interactive one to one online sessions* One faculty/student* Flexible timings * Regular/Fast tr..
Must be able to understand different types of study designs in clinical research.
Clinical training defines the need to analyze data sets such as safety analysis. With SAS, you can gain both speed and efficiency by automating repeatable clinical trial data integration. It is used for managing and verifying the industry mandated data standards such as Clinical Data Interchange Standards Consortium (CDISC). The SAS service relies on Data Integration to deliver centralized metadata management using the SAS Metadata Server. The training enhances usability by adding new metadata types and plug-ins that assist with clinically oriented tasks.
We at Benchfolks have trainers who provide clinical data management training . We have a team of expert trainers with real time experience of at least 10 years. They educate our users in the most practical ways with real time scenarios. Clinical SAS Training by trainers at Benchfolks gives you deep knowledge on course along with practical training. Once you complete full training you can master how to analyze, store and modify the data. Some trainers also provide clinical research training online for students who cannot attend the classes in person.
Clinical training course contents
Our registered trainers have designed the training for novice programmers as well as the experienced software professionals. The Clinical course covers clinical research process, Statistical Analysis Plan, classes of clinical trials data, CDISC principles and terms, regulatory requirements to export SAS data, Access DICTIONARY Tables using the SQL procedure, Apply categorization and windowing techniques to clinical trials data, Transpose SAS datasets, SAS procedures to obtain descriptive statistics, PROC REPORT to produce tables and listings for clinical trials, principles of programming validation in the clinical trial industry and Resolve data syntax and logic errors.
We are proud to say that we have the best trainers who provide the best clinical training for full real time process. We also have 100% placement support with which we have a tie up with various IT companies. SAS clinical certification is a must and should for most companies and we help to get certification and as well as skills about the course from companies that are tied up with us. You will able to learn for complete basics for Clinical certification course and programming, managing and manipulating the data process.
Refer below to select from our list of providers who provide world class training for freshers and professionals who are looking to enter the industry of Clinical research as an analyst and scientist professionals. The trainers also provide online training for users who cant attend the courses in person.
Curriculum for this Course
- Introduction to the clinical research process
- History and evolution
- Phase of clinical trials
- Protection of human subjects
- Roles of the clinical research teams
- Responsibilities of clinical research organizations
- Basic medical terminology
- Terminology associated with pharmaceutical and pharmacological research
- International regulations governing the development of drugs
- Medical devices
- And biologics.
- Review of the regulatory agencies
- Guidelines for regulatory application
- Required documentation
- Preparation for compliance audits.
- Differentiation between research design types
- Rules for writing protocols
- Ethical considerations relative to research protocols
- Correct preparation of data collection forms
- project planning
- development of study goals
- preparation of budget and contracts
- implementation of monitoring visits
- effective management of research sites
- database structures
- data management systems
- quality assurance
- data collection and capture
- data confidentiality and security
- Development of the data management plan
- Coordination of data collection and capture
- Plan the closure and archival of study materials
Development and implementation of data review and data collection the development of the validation program and the function conduct and followup of a quality assurance audit of data.
Generation of tables
Listing and graphs
The identification and reporting of data trends
Generation of various types of study reports
Jobs and Placements
Get ready for the corporate world. Take up training from the listed training companies here, and they will ensure offer you placement assistance at the end of the course. Advance your career and become an IT professional now. Enroll as a Clinical research analyst, Clinical research associate, field monitor, clinical monitor, Clinical research coordinator, Data manager, clinical research scientist, clinical quality assurance auditor or clinical safety analyst in top companies
Sample Interview Q&A
1.What is Clinical Data Management (CDM)?
Process of ensuring that the data collected during a clinical trial:
• Accurate = Conforms to truth or facts
• Logical = Legitimate
2.What Are PreClinical Studies?
Pre clinical studies are the animal studies that support Phase I safety and tolerance studies. They must comply with the GLP guidelines.
3.Explain what is SAS? What are the functions does it performs?
SAS i.e. Statistical Analysis System is a combined set of software solutions which helps user to analyze data.
• It can change, manipulate, analyze & retrieve data.
• Numerical analysis can be done.
• Report writings.
• Quality can be improved.
4.Explain what is the basic structure of SAS programing?
SAS programs consists of:
• DATA step, which recovers & manipulates data.
• PROC step, which interpret the data.
5.Name few SAS functions?
Scan, Substr, trim, Catx, Index, tranwrd, find, Sum.
The training will be a combination of theoretical and practical on each topic. The trainers will be providing live exposure on projects and give assignments to test your skill sets.
Yes, the trainer will provide you support for any clarification you need in a job.
We have 2 modes of training. Classroom Training & Online training.
All of our online courses are live instructor-led online courses. You will have the ability to interact directly with the trainer and the training is one on one too through an easy-to-use web conferencing tool like GoToMeeting etc.
The course is non-transferable to anyone else other than the person whose details are given while enrolling once the student has started
Yes, you will receive student guides from the trainers.